Alexander Rudensky, PhD, an immunologist at Memorial Sloan Kettering Cancer Center, is co-discoverer of the transcription factor FoxP3 that is essential for Treg identification and function.
Early in his career, Dr. Rudensky pursued biochemistry at Moscow’s Second Medical School, studying the interplay between the immune system’s main actors: T cells and B cells. Following postdoctoral work at Yale, he accepted a professorship at the University of Washington, where his focus turned to the molecular underpinnings of T cell development. Rudensky became particularly interested in regulatory T cells, or Tregs, thought to play a role in suppressing unwanted immune responses. The molecular identity and role of Tregs had puzzled researchers for decades, but Rudensky and his team helped solve it by discovering that the gene switch FOXP3 controls their formation.
Much of Rudensky’s career unfolded at Memorial Sloan-Kettering in New York City. Notably, he found that placental mammals form cohort of “peripheral” Tregs, and that during pregnancy, these Tregs prevent the maternal immune system from attacking the fetus, effectively linking peripheral Treg deficiency to miscarriages. Rudensky also discovered that fatty acids in the gut boost the formation of peripheral Tregs, which in turn help ward off inflammatory gut disorders, and that Tregs secrete a signaling molecule that mediates tissue repair and maintenance, establishing a central role for them in inflammation and allergies.
More recently, Rudensky and his colleagues have explored how Tregs influence cancer progression. Clinical trials involving Tregs in transplantation and autoimmune diseases are underway, and the coming years are poised to bring promising leads for cancer treatment.